Your Tasks

• Drive bio-compatibility activities across projects by providing expert assessments, guidance, and actionable recommendations
• Lead and coordinate biocompatibility strategies to ensure compliance with relevant standards and regulatory requirements
• Develop, implement, and continuously improve systems, procedures, and protocols related to biocompatibility
• Plan, execute, or coordinate testing programs and scientific justifications to demonstrate product conformity
• Act as a key interface between cross-functional teams, ensuring clear communication and alignment on biocompatibility topics

Your Profile

• Master's degree or higher degree (University, FH) in (applied) Natural Science, Toxicology or similar; experience with evaluation of biocompatibility of medical devices or comparable field in
  pharmaceuticals is strongly preferred
• Strong analytical thinking and sound, objective judgment combined with excellent written and verbal communication skills
• Proven project management experience and the ability to work effectively in interdisciplinary, cross-functional teams
• Ability to collaborate with stakeholders across multiple departments while managing priorities in a structured and efficient manner
• Professional communication style with the ability to convey complex topics clearly to diverse audiences

Further information about MED-EL can be found here.

Your Benefits

• Central Location
• Employee Discounts
• Flexible Hours
• International Environment
• Onboarding
• Workplace Well-Being

Further information

Annual gross salary from
€ 58,941.41, based on professional qualification and experience.

This position is to be filled immediately.

If you have any questions please contact Marina Engl. Central LocationEmployee DiscountsFlexible HoursInternational EnvironmentOnboardingWorkplace Well-BeingMinimum SalaryEarliest Entry DateYour Contact Person Email